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Volume: 05 Issue: 12 | Dec 2018 www.irjet.net p-ISSN: 2395-0072
© 2018, IRJET | Impact Factor value: 7.211 | ISO 9001:2008 Certified Journal | Page 1094
Conducting Poly (Aniline-Co-O-Anisidine) Coatings on Low Carbon
Steel: Synthesis, Characterization and Corrosion Protection Studies
Navalkant A. Konda1
, Laxman Khose2, Samadhan Bhosale3, Anup Chaple4
1,2,3,4
Department of Mechanical Engineering, Akurdi, Pune—411044 (M.S.), India
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Abstract:- Conducting poly (aniline-co-o-anisidine) coating
are obtained on low carbon steel sample by galvanostatic
deposition method using oxalic acid as supporting electrolyte.
The coating is characterized by UV-vis absorption
spectroscopy. The corrosion protection aspects of poly
(aniline-co-o-anisidine) co-polymer coatings on low carbon
steel were investigated in aqueous 3.5% NaCl solution by
potentiodynamic polarization studies, open circuit potential
measurements, electrochemical impedance spectroscopy and
alternate immersion testing. The results of the
potentiodynamic polarization measurement showed that the
corrosion rate of co-polymer coated steelis1.477mpywhichis
about 3 times lower than that of uncoated low carbon steel.
The electrochemical studies reveal protective nature of
electrodeposited conducting poly (aniline-co-o-anisidine)
copolymer coating even after 144 hours of immersion.
Conducting poly (aniline-co-o-anisidine) coating protectslow
carbon steel in neutral medium by preventing cathodic
reduction process.
Key Words: PANI- Polyaniline.
1. INTRODUCTION
Metals and alloys corrode in environments encountered
during their service. Corrosion can be defined as the
destruction or deterioration ofa material becauseofreaction
with its environment [1]. Perhaps, the most common
corrosion prevention method is the use of paint coatings.
Effective paint coatings contain environmentally hazardous
and toxic pigments such as strontium chromates. There is a
need to replace conventional toxic coatings by
environmental friendly and non toxic formulations.
Corrosion, being an electrochemical phenomenon, can be
tackled through the use of electrochemistry and conducting
polymers [2]. Within family of conducting polymers,
conducting polyaniline occupies an important place due to
its ease of synthesis, stability and low cost economics.
Conducting polyanilineeitherintheformofelectrodeposited
primer or in the form of paint has shown promise for
corrosion protection of active metals [3]. However, the
extent of using this polymer is limited to the exclusivity of
the monomers that are required for its synthesis. Also, its
electrochemical activity is limited due to low pH conditions
(pH < 4) required for its synthesis. Presently three methods
are used to overcome this situation – 1) The first approach
is concerned with the use of derivatives such as poly(o-
anisidine), 2) The second technique involves the formation
of bi layer coatings which either consists of a top coat
conducting polyaniline on the layer of the other conducting
polymer such as polypyrrole or a top coat of conducting
polyaniline on the metallic coating suchasnickel and3) The
third method is based on co polymerization of two
conducting polymers [4]. The aim of present work is to
synthesize conducting poly (aniline-co-o-anisidine)coatings
on low carbon steel samples by galvanostatic method, to
characterize these coatings by UV- visible spectroscopy to
study their corrosion protection performance in neutral
solution by using electrochemical methods.
poly (aniline-co-o-anisidine) copolymer coating on low
carbon steel were analytical reagents (AR Grade, supplied
by Loba Chemicals, Mumbai , India ) and used as received
(Table 1).
Table 1: Chemicals used for coating on conducting poly
(aniline-co-o-anisidine) copolymer coating on low carbon
steel sample.
Material Chemical
formula
Molecular weight
(g/mol)
Aniline C6H5NH2 93.13
o-anisidine C7H9NO 123.16
Oxalic acid C2H2O4 90.03
Low carbon steel AISI 1015 475.25
Specimen preparation
The samples for the experiments were cut from the sheet of
low carbon steel (AISI 1015). Before each experiment, the
specimen was dry polished by using a series of emery
papers. The final approximation to a flat scratch free surface
was obtained by use of the lapping machine. The specimen
was then washed under running water and dried.
2. EXPERIMENTAL WORK
Chemicals:
All chemicals required for electro deposition of conducting
2. International Research Journal of Engineering and Technology (IRJET) e-ISSN: 2395-0056
Volume: 05 Issue: 12 | Dec 2018 www.irjet.net p-ISSN: 2395-0072
© 2018, IRJET | Impact Factor value: 7.211 | ISO 9001:2008 Certified Journal | Page 1095
Galvanostatic deposition
The electrochemical deposition of conducting poly (aniline-
co-o-anisidine) coating on low carbon steel samples (AISI
1015) is carried out at room temperature in a simple one
compartment glass cell under galvanostatic conditions. A
three electrode geometry is employed during electro-
copolymerization of aniline and o-anisidine on low carbon
steel as working electrode (8 cm2), stainless steel ascounter
electrode and saturated calomel electrode (SCE) as a
reference electrode as shown in the figure 1.
Figure 1: Electrochemical Cell: A line diagram
CHARACTERIZATIONS:
The UV-Visible absorption study of electrochemically
deposited conducting co polymer coating will be carried out
ex situ in the wavelength range 200 – 1200 nm using
microprocessor controlled double beam UV-Visible
spectrophotometer (Model V 520,Jasco,Japan)todetermine
conducting phase obtained. Schematic diagram of double
beam.
UV-visible spectra of the Poly (aniline-co-o-anisidine)
copolymer were recorded at roomtemperaturein N-Methyl-
2-pyrrolidone (NMP) solution.
CORROSION PROTECTION PERFORMANCE:
A corrosion cell having three electrode geometry of paint
coatedsampleasworkingelectrode(8cm2), stainless steel
as counter electrode and saturated calomelelectrode(SCE)
asareferenceelectrodewasused.The cell wascoupledwith
Gamry Reference system 600 (Wilmington, USA) for
corrosionstudies.
RESULTS AND DISCUSSION:
Galvanostatic deposition of conducting poly (aniline-co-o-
anisidine) coating on low carbon steel sample. The UV-vis
spectrum of poly (aniline-co-o-anisidine) copolymer is
shown in the figure 2 . The copolymerization of aniline and
o-anisidine was performed under the galvanostatic
conditions. The reactivity of o anisidine is higher than
aniline, hence it seems that when the mixture of these two
monomers are polymerized more o-anisidine monomers
take part in the polymerization compared to the aniline
monomers. Consequently, there are more o-anisidine
monomeric units compared to aniline in the
electrodeposited copolymer [5].
Figure 2: UV-vis scan of conducting poly (aniline-co-o-
anisidine) copolymer electrodeposited coating.
The UV-vis spectra of poly (aniline-co-o-anisidine)
copolymer exhibit moreresemblancetothespectral features
of o-anisidine. The spectrum of copolymer is dominated by
two bands; a strong absorption band at 330- 350 nm (peak
1) and a broad band at 500-600 nm (peak 2). According to
the general practice of peak assignment, first peak is
attributed to the π-π* transition ofthebenzenoidmoietiesin
the poly (aniline-co-o-anisidine) copolymer linear structure
or simply to the band gap of the copolymer. Thesecondpeak
closely resembles the benzenoid-quinoid transition in the
copolymer. G. Bereket et.al. and MohammadReza Nabidet.al
has noted similar observations [5, 7]
CORROSION STUDIES
The Potentiodynamic polarization
Tafel curve for uncoated low carbon steel is shown in the
figure 3.
Figure 3: Tafel plot for low carbon steel sample in 3.5 wt%
NaCl.
3. International Research Journal of Engineering and Technology (IRJET) e-ISSN: 2395-0056
Volume: 05 Issue: 12 | Dec 2018 www.irjet.net p-ISSN: 2395-0072
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Potentiodynamic polarization behavior of electrodeposited
conducting co-polymer (0.05M Aniline + 0.05Mo-Anisidine)
coating on low carbon steel in 3.5 wt % NaCl solution is
depicted in the figure 4.
Figure 4: Tafel plot for of electrodeposited conducting co-
polymer (0.05M Aniline + 0.05M o-Anisidine) coating on
low carbon steel in 3.5 wt % NaCl solution.
The values of the corrosion potentials, corrosion current
densities and corrosion rates obtained fromthefigures3 &4
are recorded in Table 2.
Table 2- Corrosion rates for unpainted low carbon steel
and epoxy coated steel.
Sample Ecorr mV
Icorr
per
cm2
Corrosion
rate mpy
Uncoated low
carbon steel
-680.0
mV
87 µA 5
Co-polymer (0.05M
Aniline + 0.05 M o-
anisidine ) coated
low carbon steel
-519.0
mV
64 µA 1.477
Corrosion potential is found to be increased from – 680 mV
for uncoated low carbon steel to -519 mV for co-polymer
coated steel in noble direction. This reveals anodic type of
protection offered by co polymer. It should also be noted
that the corrosion rate is substantially reduced due to
decrease in current density from 87 µA/ cm2 to 64 µA/ cm2
for co-polymer coated steel. The corrosion rate of co-
polymer coated steel in 3.5 wt% NaCl is found to be 1.477
mpy which is about 3 times lower than that of uncoated low
carbon steel. These results are in good agreement with the
previous work [4].
3. CONCLUSION
It is possible to obtain conducting poly (aniline-co-o-
anisidine) coatings on low carbon steel sample by
galvanostatic deposition method. UV-visspectra confirmthe
copolymerization of aniline-co-o-anisidine and its
conducting phase. The corrosion rate of co-polymer coated
steel in 3.5 wt% NaCl is found to be 1.477 mpy which is
about 3 times lower than that of uncoated low carbon steel.
ACKNOWLEDGEMENT
The author thank to Dr. P. P. Deshpande for his invaluable
guidance, inspiration and support during various stages of
our research. The author also thank Prof. S.T. Vagge, Head,
DepartmentofMetallurgyandMaterialsScience,College of
Engineering, Pune—411005 (M.S.),India for providing
facilities for the work.
REFERENCES
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